Canonical Allele Identifier: CA516357994
Community Standard Title: NM_002049.4(GATA1):c.507C>T (p.Ser169=)
Gene: GATA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48792130C>T , CM000685.2:g.48792130C>T GRCh38
NC_000023.10:g.48650537C>T , CM000685.1:g.48650537C>T GRCh37
NC_000023.9:g.48535481C>T NCBI36
NG_008846.2:g.10557C>T , LRG_559:g.10557C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002049.4:c.507C>T MANE Select NP_002040.1:p.Ser169=
ENST00000376670.9:c.507C>T MANE Select ENSP00000365858.3:p.Ser169=
NM_002049.3:c.507C>T , LRG_559t1:c.507C>T NP_002040.1:p.Ser169=
ENST00000376665.4:c.507C>T ENSP00000365853.3:p.Ser169=
ENST00000376670.7:c.507C>T ENSP00000365858.3:p.Ser169=
ENST00000651144.1:c.258C>T ENSP00000498550.1:p.Ser86=
ENST00000651144.2:c.258C>T ENSP00000498550.1:p.Ser86=
ENST00000696450.1:c.507C>T ENSP00000512637.1:p.Ser169=
ENST00000696451.1:c.258C>T ENSP00000512638.1:p.Ser86=
ENST00000696452.1:c.258C>T ENSP00000512639.1:p.Ser86=
XM_011543897.1:c.507C>T XP_011542199.1:p.Ser169=
XM_011543897.2:c.507C>T XP_011542199.1:p.Ser169=
XM_011543898.1:c.258C>T XP_011542200.1:p.Ser86=
XM_011543898.2:c.258C>T XP_011542200.1:p.Ser86=
XM_024452363.1:c.258C>T XP_024308131.1:p.Ser86=